Latest Business Development Executive - Remote Jobs

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.

GSK

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. Responsibilities include managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's rare disease medicines.

Pfizer

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. This includes managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's medicines.

Pfizer

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Lead Patent Paralegal

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent

Design Engineer (Medical Devices / SolidWorks)

This role involves designing and developing medical devices from concept to design freeze, using SolidWorks to create detailed 3D models and drawings. The engineer will collaborate with manufacturing, testing, and project teams to ensure designs meet regulatory and performance standards within a structured development process. The position focuses on creating innovative healthcare products that improve young lives globally.

Ernest Gordon Recruitment Lisburn, County Antrim, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Lead .Net Developer

Lead .NET Developer – Software for Physical DevicesLocation: Remote - must be UK basedSalary: £80,000 + BonusIMPORTANT - This role focuses on building software that interfaces with and ingests data from physical devices and external systems.It is not a typical...

Technify Talent Limited United Kingdom £75,000 – £80,000 pa

Remote Permanent

Quality Engineer, Medical Devices

This role involves managing quality assurance processes within the medical devices sector, including developing documentation, conducting internal audits, and resolving customer complaints. The engineer will ensure compliance with ISO standards and support regulatory requirements in a company focused on innovative diagnostic systems. The position plays a key part in maintaining quality across a product range used in healthcare laboratories.

TRS Consulting Bolton, Manchester, M26 1HG, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Quality Engineer, Medical Devices

This role involves managing quality systems for medical devices, including creating documentation, conducting internal audits, and handling customer complaints. The engineer will ensure compliance with regulatory standards such as ISO 13485 and ISO 9001 within a leading healthcare diagnostics company. The position supports product innovation and quality assurance in a highly regulated environment.

TRS Consulting Preston, East Riding Of Yorkshire, East Riding Of Yorkshire, HU12 8SB, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Senior Software Engineer (Platform)

As a Senior Software Engineer at Owkin, you will design, implement, and maintain cloud-based infrastructure and services that support complex biomedical research and business intelligence. You will own critical platform components, drive technical standards, mentor junior engineers, and collaborate with cross-functional teams to enhance productivity and security.

Owkin United Kingdom

Remote Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent